Dejerine–Sottas disease
a rare hereditary neurological disorder characterised by damage to the peripheral nerves and resulting progressive muscle wasting
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Dejerine–Sottas disease
Summary
Dejerine–Sottas disease is a rare disease[1]. It has Wikipedia articles in 6 language editions, a strong signal of global cultural recognition.[2]
Key Facts
- Dejerine–Sottas disease's instance of is recorded as rare disease[3].
- Dejerine–Sottas disease's instance of is recorded as class of disease[4].
- Joseph Jules Dejerine is named after Dejerine–Sottas disease[5].
- Jules Sottas is named after Dejerine–Sottas disease[6].
- Dejerine–Sottas disease is a type of Charcot–Marie–Tooth disease[7].
- Dejerine–Sottas disease's Commons category is recorded as Dejerine-Sottas disease[8].
- Dejerine–Sottas disease's health specialty is recorded as neurology[9].
- Dejerine–Sottas disease's genetic association is recorded as PRX[10].
- Dejerine–Sottas disease's genetic association is recorded as PMP22[11].
- Dejerine–Sottas disease's genetic association is recorded as MPZ[12].
Why It Matters
Dejerine–Sottas disease has Wikipedia articles in 6 language editions, a strong signal of global cultural recognition.[2] It is known by 9 alternative names across languages and contexts.[13]